United States · FDA National Drug Code directory
Enalapril Maleate and Hydrochlorothiazide
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 51672-4045_5699d24d-8bf5-0759-e063-6394a90ad9a3
- Product NDC
- 51672-4045
- Form
- TABLET
- Composition / generic term
- Enalapril Maleate and Hydrochlorothiazide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010918
- Source listing expiry
- 20271231
Source-listed ingredients
- ENALAPRIL MALEATE — 5 mg/1
- HYDROCHLOROTHIAZIDE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (51672-4045-1) · 51672-4045-1
- 1000 TABLET in 1 BOTTLE (51672-4045-3) · 51672-4045-3
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →